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Clinical Trials/NCT04914988
NCT04914988
Completed
Not Applicable

Pain Management in Geriatric Hip Fracture Patients With Ultrasound-guided Continuous Fascia Iliaca Compartment Block

Mahidol University1 site in 1 country20 target enrollmentFebruary 1, 2018

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Hip Fractures
Sponsor
Mahidol University
Enrollment
20
Locations
1
Primary Endpoint
numerical rating scale at rest
Status
Completed
Last Updated
4 years ago

Overview

Brief Summary

The patient with hip fracture who has Numerical Rating Scale (NRS) ≥ 5 at rest or on movement will be indicated for USG FICB at Emergency Department or patient's ward.

The aim of this prospective observation study was evaluated the efficacy and complications of cFICB in adult hip fracture preoperatively.

Detailed Description

The Enhance Recovery Program of pain management in geriatric hip fracture has been set up as a part of fast track at Siriraj Hospital since September 2017. The ultrasound-guided (USG) fascia iliaca compartment block (FICB) is routinely offered to patients with a hip fracture by acute pain service (APS) anesthesiologist. The patient with hip fracture who has Numerical Rating Scale (NRS) ≥ 5 at rest or on movement will be indicated for USG FICB. The aim of this prospective observation study was evaluated the efficacy and complications of cFICB in adult hip fracture preoperatively.

Registry
clinicaltrials.gov
Start Date
February 1, 2018
End Date
February 15, 2019
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Suwimon Tangwiwat

Department of Anesthesiology

Mahidol University

Eligibility Criteria

Inclusion Criteria

  • patient age equal or more than 65 years old
  • patient with acute hip fracture within 7 days
  • patient with NRS ≥ 5

Exclusion Criteria

  • patient refusal
  • history of local anesthetic allergy
  • inability to communicate or cognitive dysfunction
  • multiple fracture involvement

Outcomes

Primary Outcomes

numerical rating scale at rest

Time Frame: Change from baseline numerical rating scale at 30 minutes post-block

numerical rating scale 0-10 (0=no pain, 10=worst pain)

numerical rating scale during movement

Time Frame: Change from baseline numerical rating scale at 30 minutes post-block

numerical rating scale 0-10 (0=no pain, 10=worst pain)

Secondary Outcomes

  • Duration of hospital admission(from hospital admission until hospital discharge, an average of 1 week)
  • Numerical rating scale during movement(Within 48 hours postoperative)
  • Rate of complications of continuous fascia iliaca compartment analgesia(Within 48 hours postoperative)
  • Number of participants with morbidity and mortality(6 weeks after hospital discharge)

Study Sites (1)

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